Category: Industry news

Recent，部分地区出现因饮用自制药酒而导致的中毒事件。为避免发生类似事故，食药监部门在此温馨提示： One、对餐饮单位提供自酿酒的要求： 1、餐饮单位提供自制配制酒，需具备自酿酒相关的许可条件，取得相应的许可，并在《食品经营许可证》的经营项目上标注自制饮品（自酿酒）字样。 2、餐饮服务中提供自制配制酒的，所用酒类原料应符合食品安全国家标准要求，泡制所需辅料如纳入国家药典范围的，应有传统泡制习惯，符合国家颁布的《即是食品又是药品的物质名单》、《新资源食品和新食品原料名单》要求,且不得宣称疗效。 3、餐饮单位提供的自制配制酒只限于在本门店餐饮服务中同时消费，不得单独对外销售。 Two、对广大消费者提示 1、在餐饮单位消费自制配制酒时，应注意查看餐饮单位是否持有效《食品经营许可证》经营，同时留意许可证上的经营项目是否含自酿酒字样。 2、家庭切勿随意使用药材自制药酒，特别是内服药酒。一些药材具有一定的毒性，如果未能加以认真鉴别，并按照规定进行炮制和使用，容易误用中毒。如断肠草、乌头、雪上一支蒿等中药材，具有较强的毒性，如未严格按照有关规定炮制和使用，极易引起中毒。 3、不要随便相信秘方、偏方，避免在不了解药性的情况下，盲目按秘方、偏方自制药酒使用。 4、如非必要，尽量避免家庭自制药酒。在自制药酒前，一定要详细了解有关药材的情况和制作要求。因为有些中药之间药性相克，一起浸泡有可能产生毒素，在自制前，一定要咨询有关医生或者药师。尽量避免自行采摘药材进行泡制，也不可随意在街边或旅游点采购中草药进行泡制，一定要从正规渠道购买药材，以确保健康和生命安全。 5、药酒并不是任何人都适合饮用的，也不是可以无限量、无期限地服用，一定要根据自己的年龄、体质来选择，而且药酒也不宜过量饮用。市民一旦发生饮用自制药酒中毒，要及时前往医院救治。

各市人民政府，省安委会成员单位，中央在浙和省属有关企业： 为认真贯彻《国务院安委会关于印发安全生产约谈实施办法（试行）的通知》（安委〔2018〕2号）要求，进一步深化我省安全生产领域改革发展，强化安全生产责任落实，省安委会研究制定了《浙江省安全生产通报警示约谈实施办法（试行）》。With the consent of the provincial government，现印发给你们，Please take it seriously。 浙江省安全生产委员会 2018年6月25日 浙江省安全生产通报警示约谈实施办法（试行） 第一章　总 则 第一条　为进一步加强安全生产工作，强化责任落实，有效预防和减少各类生产安全事故（生产安全事故以下简称“事故”）发生，根据《中华人民共和国安全生产法》《浙江省安全生产条例》和《地方党政领导干部安全生产责任制规定》、《国务院安委会关于印发安全生产约谈实施办法（试行）的通知》（安委〔2018〕2号）、《中共浙江省委 浙江省人民政府关于深入推进安全生产领域改革发展的实施意见》（浙委发〔2017〕35号）等法律法规和政策规定，These measures are formulated。 第二条　本办法所称安全生产情况通报，是指省安委会办公室就全省阶段性事故情况和安全生产工作情况向设区市政府、省级有关部门或中央在浙和省属有关企业（以下简称省部属企业）进行通报。 本办法所称安全生产警示，分为安全生产警示通报和警示告知，是指省安委会就省内发生的有较大社会影响等事故，或就存在的区域性、行业性安全生产问题，分别对各设区市政府、省级有关部门、省部属企业进行预警性警示通报和督促性警示告知。 本办法所称安全生产约谈，是指省安委会对未履职、履职不到位或发生重大社会影响事故的设区市政府、省级有关部门和省部属企业的主要负责人或分管负责人进行提醒、告诫，督促整改的谈话。 第二章　安全生产情况通报 第三条　根据国家统计有关规定，省安委会办公室每月统计汇总各类事故（包括工矿商贸企业、道路运输、水上运输、渔业船舶、铁路运输）情况，向省委、省政府有关领导和省级有关部门、各设区市安委会通报。 第四条　省安委会办公室根据全省安全生产工作情况，对全省开展的安全专项整治、安全生产大检查、重大事故隐患挂牌整治、年度安全生产目标管理责任制考核，以及上级部门要求督办的安全生产工作和较大以上的事故责任追究等情况，向各设区市政府、省级有关部门或省部属企业通报；同时抄送省委、省政府有关领导，以及省监委和省委组织部等。 第三章　安全生产警示 第五条　对省内发生的有较大社会影响、较典型的较大事故，重大及以上事故，以及敏感时期发生的事故，由省安委会及时向各设区市政府、省安委会各成员单位进行警示通报。对发生的典型行业性的较大事故或有重大影响的一般事故，由行业部门及时向全省该行业领域及企业进行警示通报。 通报内容包括事故经过及初步原因、事故教训、防止同类事故发生的针对性措施等要求。 第六条　有下列情形之一的，省安委会将对所在设区市政府、省级有关部门或省部属企业进行安全生产警示告知： （一）存在行业性、区域性事故隐患和突出问题的； （二）安全生产工作不到位，出现监管盲区或非法违法行为长期存在的； （三）60天内重复发生同类型较大事故，省部属企业发生同类型一般事故的； （四）事故控制不力，事故总量同比上年度上升的； （五）较大以上事故责任追究超过半年未落实的； （六）未按要求完成上级重大工作部署的； （七）省安委会认为需要警示告知的其他情形。 第七条　对符合警示告知情形的单位，由省安委会办公室拟定警示告知书，报省安委会领导审定签发，同时抄送省监委、省委组织部、省政府办公厅；省部属企业还应抄送该企业上级主管部门或总公司。 第八条　被警示告知的设区市政府、省级有关部门或企业应自接到警示告知之日起15日内，以书面形式将存在的主要问题及原因、防范整改措施落实情况报送省安委会办公室。 第四章　安全生产约谈 第九条　符合第十、Eleven、十二条情形的，应当实施约谈，组织实施约谈的具体工作由省安委会办公室承办。 第十条　发生特别重大事故的，由省安委会主任对设区市党政主要领导，省级有关部门（省部属企业）主要负责人进行约谈。 第十一条　有以下情形之一的，由省安委会主任或指派的副主任对设区市政府、省级有关部门（省部属企业）主要负责人或分管负责人，以及事故发生地县（市、区）党委、政府主要负责人进行约谈。 （一）发生重大事故的； （二）事故应急处置不力，致使事故危害扩大，死亡人数达到重大事故的； （三）1年内2次以上被警示告知，或被警示后仍未按要求整改、问题依然突出的； （四）省安委会认为需要约谈的其他情形。 第十二条　有以下情形之一的，由省安委会办公室主要负责人或指派的负责人进行约谈。 （一）6个月内发生3起较大事故； （二）30天内发生2起以上较大事故的； （三）发生危化品泄漏或爆炸等事故，造成重大社会影响的；或发生性质严重、社会影响恶劣较大事故的； （四）事故应急处置不力，致使事故危害扩大，达到较大事故的； （五）中央或省督办的较大事故未按要求完成调查，或未落实责任追究、防范和整改措施的； （六）国务院安委办督办的重大事故隐患，未按要求完成整改的； （七）省安委会认为需要约谈的其他情形。 设区市政府有前款第一至第七项情形之一的、省级有关部门和省部属企业有前款第三至第七项情形之一的，由前款规定的相应约谈人对设区市政府、省级有关部门（省部属企业）分管负责人进行约谈。 第十三条　约谈程序的启动： （一）省安委会进行的约谈，由省安委会办公室提出建议，报省安委会领导同志审定后，启动约谈程序； （二）省安委会办公室进行的约谈，由省安委会有关成员单位按工作职责提出建议，报省安委会办公室主要负责人审定后，启动约谈程序； （三）省安委会成员单位进行的约谈，由本部门有关内设机构提出建议，报本部门分管负责人批准后，启动约谈程序。 第十四条　约谈经批准后，由约谈方书面通知被约谈方，告知被约谈方约谈事由、Time、place、procedure、参加人员、需要提交的材料等。 第十五条　被约谈方应根据约谈事由准备书面材料，主要包括基本情况、Cause analysis、主要教训以及采取的整改措施等。 第十六条　约谈方除主约谈人和组织约谈的相关人员外，省安委会办公室视情邀请相关单位负责人参加约谈。 被约谈方除第十条、Article 11、第十二条规定的相关人员外，省安委会办公室可视情要求有关企业主要负责人接受约谈。 第十七条　约谈实施程序： （一）约谈方说明约谈事由和目的，通报被约谈方存在的问题； （二）被约谈方就约谈事项进行陈述说明，提出下一步拟采取的整改措施； （三）讨论分析，确定整改措施及时限； （四）形成约谈纪要。 省安委会成员单位进行的约谈，约谈纪要抄送省安委会办公室。 第十八条　整改措施落实与督促： （一）被约谈方应当在约定的时限内将整改措施落实情况书面报约谈方，约谈方对照审核，必要时可进行现场核查； （二）落实整改措施不力，连续发生事故的，由约谈方给予通报，并抄送被约谈方的同级党委和上一级监委，依法依规严肃处理。 第十九条　约谈方根据政务公开的要求及时向社会公开约谈情况，Accept social supervision。 第二十条　省安委会有关成员单位、各设区市安委会可参照本办法制定本单位、本地区安全生产通报警示约谈办法。 第五章　附　则 第二十一条　设区市政府、省级有关部门和省部属企业整改落实警示告知或约谈事项的情况纳入省政府安全生产目标管理责任制考核内容。年内被警示、约谈2次以上的单位，当年安全生产目标管理责任制考核不得评为优秀和良好等次。 Read More …

2015year，The U.S. Food and Drug Administration (FDA) has successively promulgated supporting regulations of the FDA Food Safety Modernization Act (hereinafter referred to as FSMA).，For food products sold in the United States，A series of new requirements have been put forward by overseas production and processing enterprises and their importers, including imported food。Recent，Some regulations will come into force，In order to avoid the impact on the export business of China's food enterprises to the United States，The following is an announcement of the relevant matters related to the relevant laws and regulations： One、Relevant Regulatory Compliance Requirements and Compliance Dates Current Good Manufacturing Practices for Human Food，Hazard Analysis and Risk-Based Preventive Controls (21CFR117)、Cultivation of agricultural products for human consumption、harvest、Packaging and storage standards(21CFR112)》、"Foreign Supplier Verification Program"、U.S. FSMA regulations, such as Mitigation Strategies to Protect Food from Intentional Adulteration, have different compliance dates for different business categories and business sizes，See the attachment for details。 Two、Related Businesses、Institutions should do a good job of responding to laws and regulations Each company exporting to the United States should consider its own scale and the situation of exporting American products，Know exactly when you will be compliant with the regulations，Establish and implement a HACCP system and Food Defense Plan (FDP) that comply with FDA/FSMA regulations，Keep your FDA registration up to date，It also reminds and cooperates with U.S. importers to implement their verification responsibilities in accordance with the requirements of the Foreign Supplier Verification Program and the Voluntary Qualified Importer Program。 The National Food Safety HACCP Application Research Center of the Chinese Academy of Inspection and Quarantine (hereinafter referred to as the National HACCP Center) has long cooperated with the CNCA to carry out FSMA response work，It has completed the compilation of the series of books on the response of export food enterprises to the FSMA of the United States，Relevant enterprises and professional institutions can directly contact and consult。The National HACCP Center and other relevant professional institutions should continue to do a good job in the research and translation of relevant laws and regulations、Guidelines for writing、Inquiries and Q&A、Relevant training、Personnel training and capacity building，And actively help enterprises to do a good job of registration notification、Audit, validation, and readiness to receive FDA on-site inspections，Assist enterprises to solve problems such as obstruction of import customs clearance in a timely manner。Encourage relevant professional bodies to establish coordination mechanisms，Coordinate the implementation of relevant response and capacity building work。Encourage all professional institutions to communicate with the CNCA in a timely manner and report on their work。 Three、Consultation Channels Consultation and emergency rescue calls from the National HACCP Center：010-53897259、010-53897273，mailbox：wangx@caiq.gov.cn，Contact：Wang Xin、Yang Qian。 The contact number of the Registration Management Department of CNCA：010-82260740，mailbox：leixj@cnca.gov.cn，Contact：Lei Xiaojuan。 The announcement is hereby made。 annex：FSMA compliance requirements and compliance dates

6May 22nd，Jiangsu Provincial Bureau of Quality Supervision released the results of sampling inspection of glasses。Fitting glasses is a tool for correcting refractive errors，It is mainly processed and produced by glasses retail enterprises。A total of 186 batches of products were randomly inspected，Qualified 176 batches，The pass rate is 94.6%。 Spot checks found，6The spherical top power item of the batch product is unqualified、1The cylindrical top power item of the batch product is unqualified。Spherical top power deviation、The cylindrical top power deviation reflects the basic luminosity characteristics of the lens，It is also a functional indicator of its corrective vision。A large deviation in the top power of the spherical lens and the top power of the cylindrical lens is equivalent to increasing or decreasing the patient's refraction，As a result, the top power of the glasses does not match the diopter required by the patient，The patient's eyes are in a state of undercorrection or overcorrection for a long time，Produces eye strain。 Spot checking，2The optical center level deviation item of the batch product is not qualified、2The one-sided horizontal deviation of the optical center of the batch product is unqualified，When worn, it will produce a prismatic effect in front of the eyes，Causes strabismus or other functional impairment of the eye。thereinto，The optical center horizontal deviation is the difference between the measured value of the horizontal distance of the optical center and the nominal value (interpupillary distance).，Unilateral horizontal deviation of optical center is the difference between the measured value of the horizontal unilateral distance of the optical center and the nominal value (unilateral interpupillary distance).。 furthermore，1The cylindrical mirror axial deviation item of the batch product is unqualified。This item is necessary to prescribe correction of astigmatism in the eye，It is directly related to vision correction and wearing effect。The deviation is too large，As a result, the direction of the axis of the spectacle column (i.e., astigmatism) does not coincide with the axis of the cylinder (astigmatism) of the spectacle fitter，Phenomena such as double vision occur when visualizing。There was also 1 batch of products that failed the assembly quality project，There is a noticeable gap in the glasses，This will lead to a reduction in the service life of the product，and affect the aesthetics and comfort of the product。 The quality supervision department recommends that consumers buy，Choose a qualified fitting shop。Check if the fitting shop has a business license and other necessary documents，Whether there is a necessary environment for optometry and glasses，optometrist、Whether the fixed distribution worker has the corresponding professional certificate qualification。Pay attention to the quality of the spectacle frame and spectacle lens，Look at the lenses、Whether the frame has been obtained and affixed with the "QS" quality and safety mark，Whether the outer packaging has a certificate of conformity、Factory name and address、Contact number、Execution standards and other information；The actual surface of the lens should be smooth and clean、Perspective is clear、Uniform color、No blemishes and visible scratches；The frame plating should be shiny，The surface should be wrinkle-free、No corrosion spots, discoloration, etc。 Good quality glasses should be seen clearly after wearing、comfortable、long。Spectacle assembly、After adjustment，You can put on your glasses and take a walk，Look far、Close-up，Whether there is dizziness、disgusting、Eye pain and seeing if the ground is flat、Whether the fixed object is tilted or not。If you feel dizzy while wearing it，dim eyesight，Visual fatigue such as tears，You should take off your glasses and go outside to rest in time，In the exclusion of ocular diseases，Bad eye habits and other factors，Check whether there is a quality problem with the glasses in time。 The list of glasses product quality supervision and random inspection enterprises and the results .xls

6On the afternoon of the 20th of the month，The CNCA and the Administrative Committee of the Shanghai Pilot Free Trade Zone signed a memorandum of cooperation on jointly promoting the certification, accreditation, inspection and testing of the Pilot Free Trade Zone。Qin Yizhi, deputy director of the State Administration for Market Regulation，Member of the Standing Committee of the Municipal、Secretary of the Pudong New Area Party Committee、Weng Zuliang, Director of the Management Committee of the Shanghai Pilot Free Trade Zone，Deputy Secretary of the Party Leadership Group of CNCA、Deputy Director Liu Weijun，Secretary of the Party Leadership Group of Shanghai Municipal Bureau of Quality and Technical Supervision、Director Huang Xiaolu，Zhu Ming, deputy director of Shanghai Municipal Bureau of Quality and Technical Supervision，Lu Mei, director of China Quality Certification Center，Member of the Standing Committee of Pudong New Area Party Committee、Deputy District Chief、Lu Fangzhou, Deputy Director of the Administrative Committee of the Shanghai Pilot Free Trade Zone, attended the signing ceremony。Secretary of the Party Committee of Pudong New Area Market Supervision Bureau (Quality Development Bureau).、Director Wu Weiping presided over the event。 Qin Yizhi promoted the cooperation between the two sides to take root、Achieve real results，Three points were made：First, it is necessary to summarize the successful experience of the pilot free trade zone，Further play a good role in certification and accreditation。Second, it is necessary to accelerate the construction of quality certification system，Better serve the reform and opening up of the pilot free trade zone。It is necessary to further optimize the supply system，Support the reform of "decentralization, decentralization and service" in the free trade zone；It is necessary to strengthen the platform carrier，Promote the high-quality development of free trade zones；It is necessary to improve the ability to innovate，Serve the construction of the National Science and Technology Innovation Center；It is necessary to deepen international cooperation，Enhance the "bridgehead" effect of opening up to the outside world。Third, it is necessary to enhance two-way synergy，Jointly promote the implementation of the memorandum of cooperation。 Weng Zuliang said，Pudong will make greater efforts to promote the development of inspection, testing and certification，Provide strong support for Pudong to build a strong quality area，Focus on building inspection, testing and certification services、cooperate、innovation、"Four New Highlands" of Industry。 will be there，Liu Weijun、Lu Fangzhou signed a memorandum of cooperation on behalf of the CNCA and the Administrative Committee of the Shanghai Pilot Free Trade Zone。The memorandum of cooperation is clear，CNCA will support the Shanghai Free Trade Zone to build a communication platform with foreign inspection, testing and certification institutions，Promote the acceptance of inspection and testing results and mutual recognition with certification bodies，Improve the level of trade facilitation of market players，Help enterprises deal with foreign technical barriers，Provide certification and accreditation policies、technology、Focused support of information，Provide inspection and testing for Chinese enterprises, including import and export related inspections、Accreditation and accreditation、Standard measurement and other services，Help enterprises better "go global"。 Huang Xiaolu and Lu Mei inaugurated the "Belt and Road" International Cooperation Center for Technology Exchange in the Shanghai Pilot Free Trade Zone。 The person in charge of the relevant department of the Municipal Bureau of Quality and Technical Supervision、The main person in charge of the member units of the Pudong New Area Quality Work Leading Group、The governing units of the Inspection, Testing and Certification Industry Association attended the meeting。